Phenotype #0000274648

Individual ID 00380795
Associated disease LGMDR10;LGMD2J
Phenotype details delayed motor development; muscular hypotonia; lactic acidosis (Neurological)
Diagnosis/Initial -
Inheritance Familial
Diagnosis/Definite LGMD type 2J
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-08-23 12:15:23 +02:00 (CEST)
Date last edited N/A

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